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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06332482
Other study ID # M0303023RP
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 30, 2023
Est. completion date September 15, 2024

Study information

Verified date March 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will compare the occlusal accuracy of different techniques for recording maxillomandibular relationships in a Complete digital workflow to construct full arch implant-supported screw-retained restoration.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 10
Est. completion date September 15, 2024
Est. primary completion date May 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria: - • Inclusion criteria: i- complete maxillary and mandibular edentulous arches ii- residual alveolar ridges covered with healthy firmly attached mucosa. iii- Angel's class I maxillo-mandibular relationship and iv- Adequate bone height and width for placement of standard diameter implants. Exclusion Criteria: - History of drug administration that interfere with bone quality ii- Surgical contraindication (patients under anticoagulant ,immunosuppressive drugs, chemotherapy and irradiation therapy) iv- tempromandibular or myoneurological disorders.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Implant supported screw retained prosthesis
All patients will receive six maxillary and mandibular implants for full arch screw retained prosthesis

Locations

Country Name City State
Egypt Mansoura University ,Faculty of dentistry Mansoura

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary measurement of occlusal prematurity Occlusal prematureties of final prosthesis will be measured using occlusense device one year
Primary prosthestic complications prosthetic complications will be recorded for all patients and statistically analyzed one year
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